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Prenatal Diagnosis|October 1, 1988
Prenatal diagnosis of cystic fibrosis using linked DNA probesM Schwartz, M Super, J Schmidtke, et al.American Journal of Medical Genetics|June 15, 1994
Search for linkage to schizophrenia on the X and Y chromosomesL E DeLisi, M Devoto, R Lofthouse, et al.Human Mutation|January 1, 1992
Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypesL Cremonesi, M Ferrari, E Belloni, et al.Human Genetics|August 1, 1990
Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8M Dean, J A Amos, J Lynch, et al.Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.Gene Geography : a Computerized Bulletin on Human Gene Frequencies|April 1, 1990
Regional distribution of cystic fibrosis linked DNA haplotypes in Italy, a collaborative studyP Gasparini, N Cappello, B Dallapiccola, et al.Human Genetics|November 1, 1990
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in ItalyI Dianzani, M Devoto, C Camaschella, et al.Human Mutation|January 1, 1995
Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian populationM P Russo, G Romeo, M Devoto, et al.Molecular Medicine (Cambridge, Mass.)|May 1, 1996
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritanceL D Spotila, J Caminis, M Devoto, et al.American Journal of Human Genetics|October 1, 1988
Recombinations between IRP and cystic fibrosisM Farrall, B J Wainwright, G L Feldman, et al.Pageof 8